Hypertension is a major public health concern affecting over 1 billion people worldwide. It is a leading cause of death and its prevalence is increasing. The document discusses guidelines for defining and classifying hypertension from organizations like JNC and WHO. It also summarizes lifestyle modifications and pharmacological treatments recommended for managing hypertension, including initial drug classes like ACE inhibitors, ARBs, calcium channel blockers, and thiazides. The guidelines emphasize starting with one drug and titrating dosage before adding additional medications to control blood pressure.
Hypertension is also known as high blood pressure. There are mainly two type of blood pressure i.e. systolic and another one is diastolic . The hypertension are categories into two parts that is primary hypertension and secondary hypertension. People are suffering from 3 stage during the condition of hypertension. There are following agents are used to treat hypertension like calcium channel blockers, ACE inhibitors, beta blocker, alpha + beta blockers these are commonly used.
This lecture presents the 1-Updated recommendations regarding definition and proper diagnosis of HTN. 2-Updated guidelines for threshold of BP to start treatment and targets of treatment. 3- Updated recommendations on CV risk assessment and management. 4-Hypertension and comorbidities: updated guidelines
The Progression of Hypertensive Heart Disease.From hypertension to heart failuremagdy elmasry
Staging of Hypertensive Heart Disease.Precipitants and clinical sequelae related to LVH and myocardial fibrosis.Imaging in hypertensive heart disease .Differential diagnosis of LVH.Concentric LVH .Eccentric LVH . Concentric remodeling .linking hypertension and atrial fibrillation
Management of hypertensive condition in 2020 according to AHA/ASA guidelines. We will discuss the presentation, clinical assessment, investigations, and management of hypertension along with major randomized controlled trials and guidelines.
Case history
Definition & incidence of Hypertension
Classification of Hypertension
Diagnosis/ Confirmation of Hypertension
Technique of Hypertension Measurement
White coat Hypertension
Type of Hypertension
Suspicion of secondary hypertension
Management of Hypertension(Stage 1& 2)
Why treatment is necessary
Life style modification
Drug treatment of Hypertension
Rationalae of combination
Hypertension management in special situation/ with complications
La Dra. Ainara Lozano Bahamonde repasa las novedades incluidas en las últimas guías europeas en insuficiencia cardiaca presentadas en ESC Congress 2021.
1. Resistant Hypertension, complications, Target organ damage2. newly diagnosed stage-1 hypertension, rationale of use of ARB and comparison of Azilsartan with other ARBs3. Hypertension with bronchial asthma 4. Hypertension with Diabetes Mellitus with proteinuria5. Hypertension , Diabetes and IHD6. Gestational Hypertension , rationale of use of drugs7. Hypertension , Diabetes , ACS8. Hypertension, Diabetes and Syndrome X9. Hypertension and special situations
application of epidemiology in htn in community.pptxanjalatchi
Hypertension is when blood pressure is too high. Blood pressure is written as two numbers. The first (systolic) number represents the pressure in blood vessels when the heart contracts or beats. The second (diastolic) number represents the pressure in the vessels when the heart rests between beats.
Hypertension is also known as high blood pressure. There are mainly two type of blood pressure i.e. systolic and another one is diastolic . The hypertension are categories into two parts that is primary hypertension and secondary hypertension. People are suffering from 3 stage during the condition of hypertension. There are following agents are used to treat hypertension like calcium channel blockers, ACE inhibitors, beta blocker, alpha + beta blockers these are commonly used.
This lecture presents the 1-Updated recommendations regarding definition and proper diagnosis of HTN. 2-Updated guidelines for threshold of BP to start treatment and targets of treatment. 3- Updated recommendations on CV risk assessment and management. 4-Hypertension and comorbidities: updated guidelines
The Progression of Hypertensive Heart Disease.From hypertension to heart failuremagdy elmasry
Staging of Hypertensive Heart Disease.Precipitants and clinical sequelae related to LVH and myocardial fibrosis.Imaging in hypertensive heart disease .Differential diagnosis of LVH.Concentric LVH .Eccentric LVH . Concentric remodeling .linking hypertension and atrial fibrillation
Management of hypertensive condition in 2020 according to AHA/ASA guidelines. We will discuss the presentation, clinical assessment, investigations, and management of hypertension along with major randomized controlled trials and guidelines.
Case history
Definition & incidence of Hypertension
Classification of Hypertension
Diagnosis/ Confirmation of Hypertension
Technique of Hypertension Measurement
White coat Hypertension
Type of Hypertension
Suspicion of secondary hypertension
Management of Hypertension(Stage 1& 2)
Why treatment is necessary
Life style modification
Drug treatment of Hypertension
Rationalae of combination
Hypertension management in special situation/ with complications
La Dra. Ainara Lozano Bahamonde repasa las novedades incluidas en las últimas guías europeas en insuficiencia cardiaca presentadas en ESC Congress 2021.
1. Resistant Hypertension, complications, Target organ damage2. newly diagnosed stage-1 hypertension, rationale of use of ARB and comparison of Azilsartan with other ARBs3. Hypertension with bronchial asthma 4. Hypertension with Diabetes Mellitus with proteinuria5. Hypertension , Diabetes and IHD6. Gestational Hypertension , rationale of use of drugs7. Hypertension , Diabetes , ACS8. Hypertension, Diabetes and Syndrome X9. Hypertension and special situations
application of epidemiology in htn in community.pptxanjalatchi
Hypertension is when blood pressure is too high. Blood pressure is written as two numbers. The first (systolic) number represents the pressure in blood vessels when the heart contracts or beats. The second (diastolic) number represents the pressure in the vessels when the heart rests between beats.
SYSTEMIC HYPERTENSION AND SCOPE OF HOMOEOPATHY
Dr. Smita Brahmachari
Abstract:
Hypertension (HTN) is an enormous health problem and is one of the biggest health challenges in the 21st century. Although the condition is common, readily detectable, and easily treatable, it is usually asymptomatic and often leads to lethal complications if left untreated. The prevalence of HTN is increasing rapidly in India driven by diverse health transitions. Apart from health implications it has huge societal, developmental and economic costs to resource constrained health systems, particularly developing nations like India. Further, hypertension is also a leading cause for hospitalizations and outpatient visits.
Reducing systolic and diastolic BP can decrease cardiovascular risk and this can be achieved by non-pharmacological (lifestyle measures) as well as pharmacological means (medicines). Homoeopathic system of medicine particularly individualized constitutional approach has significant beneficial effects on patients suffering from HTN and thus widely used in length and breadth of our nation as an alternative public health approach in curbing the increasing prevalence of HTN because of its cost effectiveness and minimal side effects.
In current scenario with rising burden of HTN posing a serious health threat to health care system of India, the present article makes a sincere attempt to present before its readers how to timely and effectively address a case of HTN at primary level health care set-up with homoeopathic medicines.
Author : The author has done her post-graduation from National Institute of Homoeopathy, Kolkata in the subject Homoeopathic Repertory. She is presently working as Medical Officer in Dept. of ISM &Homoeopathy under Govt. of NCT Delhi.
E-mail id: smita.brahmachari@rediffmail.com.
HypertensioN, The Silent Killer, Hypertension is a common disease that is simply defined as persistent elevated arterial blood pressure (BP).
Hypertension (HTN), also known as high blood pressure (BP), affects millions of people. High blood pressure is defined as BP ≥140/90 millimeters of mercury (mmHg). As per JNC 8
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
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Acute scrotum is a general term referring to an emergency condition affecting the contents or the wall of the scrotum.
There are a number of conditions that present acutely, predominantly with pain and/or swelling
A careful and detailed history and examination, and in some cases, investigations allow differentiation between these diagnoses. A prompt diagnosis is essential as the patient may require urgent surgical intervention
Testicular torsion refers to twisting of the spermatic cord, causing ischaemia of the testicle.
Testicular torsion results from inadequate fixation of the testis to the tunica vaginalis producing ischemia from reduced arterial inflow and venous outflow obstruction.
The prevalence of testicular torsion in adult patients hospitalized with acute scrotal pain is approximately 25 to 50 percent
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
3. Hypertension is a silent, invisible killer that
rarely causes symptoms. Increasing public
awareness is key, as is access to early detection.
Raised blood pressure is a serious warning sign
that significant lifestyle changes are urgently
needed. People need to know why raised blood
pressure is dangerous, and how to take steps to
control it. Dr Margaret Chan
4. Hypertension is defined as a systolic
blood pressure equal to or above 140
mm Hg and/or diastolic blood pressure
equal to or above 90 mm Hg
4
5. The new Hypertension Guideline changes the
definition of hypertension, which is now considered
to be any systolic BP measurement of 130 mm Hg or
higher—or any diastolic BP measurement of 80 mm
Hg or higher.
14. Frequently asymptomatic until severe and target
organ disease has occurred
Fatigue, reduced activity tolerance
Dizziness/Headache
Palpitations,
Angina
Dyspnoea
15. § Sleep apnea
§ Drug-induced or related causes
§ Chronic kidney disease
§ Primary aldosteronism
§ Renovascular disease
§ Chronic steroid therapy and Cushing’s syndrome
§ Pheochromocytoma
§ Coarctation of the aorta
§ Thyroid or parathyroid disease
19. History
Family history
Life style (exercise, salt intake, smoking, alcohol)
Drug history
Symptoms of secondary hypertension
(pheochromocytoma - paroxysmal headache, palpitation,
sweating )
Symptoms of complication (angina, breathlessness)
20. Examination
Radio-femoral delay in coarctation of aorta
Enlarged kidneys in Polycystic kidney
disease
Abdominal bruits in renal artery stenosis
Characteristic face for Cushing's syndrome
Abnormal optic fundi
Apical heave(Left ventricular hypertrophy)
Accentuation of the aortic component of the
second heart sound,
Fourth heart sound
Evidence of generalised atheroma or specific
complications, such as aortic aneurysm or
peripheral vascular disease.
24. Threshold of intervention:
JNC-8: when should we initiate treatment:
Age:>60years
SBP≥150-mmHg
DBP≥90-mmHg
Age:<60years
SBP≥140mmHg
DBP≥90mmHg
Strong recommendation to reduce stroke, heart failure ,
coronary heart disease.
25. Threshold of intervention:
ASH guideline:
Age:>80 years
BP-150/90 mmHg
Age<80 years
BP-140/90 mmHg
Uncomplicated stage-1 HTN
Consider 6 -12 month lifestyle change before starting
pharmacotherapy.
26. Globally cardiovascular disease
accounts for approximately 17
million deaths a year, nearly one
third of the total deaths. Of these,
complications of hypertension
account for 9.4 million deaths
worldwide every year .
Hypertension is responsible for at
least 45% of deaths due to heart
disease and 51% of deaths due to
stroke .
26
27. In terms of attributable
deaths, hypertension is one of
the leading behavioral and
physiological risk factor to which
13% of global deaths are
attributed.
Hypertension is reported to
be the fourth contributor to
premature death in developed
countries and the
seventh in developing
countries.
27
28. Recent reports indicate that nearly
1 billion adults (more than a
quarter of the world’s population)
had hypertension in 2000, and
this is predicted to increase to
1.56 billion by 2025.
Today, mean blood pressure
remains very high in many African
and some European countries.
The prevalence of raised blood
pressure in 2008 was highest in
the WHO African Region at 36.8%
.
28
29. Hypertension (HTN) is a major public health concern, affecting 26%
of adults worldwide1
Number of
people with HTN
worldwide in 20001
972 million
Increase in the
number of adults with
HTN globally by 20251
60%
Percent of all global
healthcare spending
attributable to high
blood pressure2
10%
Annual worldwide cost of
hypertension2$370 billion
1. Kearney PM, Whelton M, Reynolds K, Muntner P, Whelton PK, He J. Global burden of hypertension: analysis of worldwide data. Lancet. 2005 Jan 15-21;365(9455):217-23. Gaziano TA, Asaf B, S Anand, et.al. The
global cost of nonoptimal blood pressure. J Hypertens 2009; 27(7): 1472-1477.
1.6 Billion
HTN patients estimated
by 2025
30. Global Burden of Hypertension
2025 Projection
26.4%of world adult
population had
hypertension
Total of 972 million
adults
establishedmarket
economies(eg, North
• Total of 1.56 billion adults
20 %in developed nations,
80% in developing nations)
Highest prevalence is in• Highest prevalence will be in
developingcontinents (eg, Asia,
Africa) will account for 75% of
world’s hypertensive patients
Year2000 Year2025
• 29.2%of world adult
population will have
hypertension
America, Europe)
Kearney PM et al. Lancet. 2005;365:217-223. 19
31. 31
According to the Bangladesh NCD Risk Factor
Survey 2010, the prevalence of hypertension is
17.9% in general, 18.5% in men and 17.3% in
women
A Systematic review reported that around 14%
Bangladeshi adults suffer from hypertension.
A study in rural and semi urban surveillance sites
of icddr’b found the prevalence of hypertension to
be more than double that of in the semi-urban
population (24%) compared to the rural
population (11%)
Hypertension: Epidemiology in BD
Ref: BANGLADESH HEALTH WATCH REPORT 2016 Bangladesh Heart Journal Vol. 31, No. 2, July 2016
32. In Bangladesh:
WHO and BSM-NCD survey 2010-17.8%
Hypertension center Rangpur: 33.3%
Demographic reports: 24.4%
Hypertension: Epidemiology in BD
According to the Health Bulletin 2015, CVD and stroke
together was the topmost cause of death in Upazila,
District and Medical College Hospitals, and was
responsible for 17.78%, 21.83% and 16.32% deaths
respectively in 2014.
Ref: BANGLADESH HEALTH WATCH REPORT 2016 Bangladesh Heart Journal Vol. 31, No. 2, July 2016
33. Prevalence of hypertension (blood pressure>140/90
mmHg or drug treatement) in urban and rural areas
in Bangladesh
Hypertension: Epidemiology in BD
BANGLADESH HEALTHWATCH REPORT 2016REf;
39. 2013 ESH/ESC Guidelines for the management of arterial hypertension
The Task Force for the management of arterial hypertension of the European Society of Hypertension (ESH) and of the European Society of Cardiolo
Powered by
gy (ESC) - J Hypertension 2013;31:1281-1357
Lifestyle changes for hypertensive patients
* Unless contraindicated. BMI, body mass index.
Recommendations to reduce BP and/or CV risk factors
Salt intake Restrict 5-6 g/day
Moderate alcohol intake Limit to 20-30 g/day men,
10-20 g/day women
Increase vegetable, fruit, low-fat dairy intake
BMI goal 25 kg/m2
Waist circumference goal Men: <102 cm (40 in.)*
Women: <88 cm (34 in.)*
Exercise goals ≥30 min/day, 5-7 days/week
(moderate, dynamic exercise)
Quit smoking
40. Patient education about treatment
Assess the patient’s understanding and acceptance of the
diagnosis of hypertension.
Discuss patient’s concerns, and clarify misunderstandings.
Tell the patient the blood pressure reading, and provide a
written copy.
Come to agreement with the patient on goal blood
pressure.
Ask the patient to rate from 1 to 10 his or her chance of
staying on treatment.
41. Patient education about treatment
Inform the patient about recommended treatment, and provide
specific written information about the role of lifestyle including diet,
physical activity, dietary supplements, and alcohol intake; use
standard brochures when Available
Elicit concerns and questions, and provide opportunities for the
patient to state specific behaviors to carry out treatment
recommendations.
Emphasize:
• Need to continue treatment
• Control does not mean cure
• One cannot tell if blood pressure is elevated by “feeling
or symptoms”; blood pressure must be measured
44. Treatment Regimen
Most of the patients need more than
one drug to achieve control of blood
pressure
Increase the dose of drug or add new
drugs at 2-4wks interval.
If the untreated blood pressure is
20/10mmHg above target blood
pressure, consider treatment
immediately with 2drugs.
46. JNC 8
• 2014 Evidence-Based Guidelines for
the Management of High Blood
Pressure in Adults
– JAMA. 2014;311(5):507-520
From: 2014 Evidence-Based Guideline for the Management of High Blood Pressure
in Adults: Report From the Panel Members Appointed to the Eighth Joint National
Committee (JNC 8)
JAMA. 2014
47. JNC 8 Recommendations
• JNC7 published in 2003, IOM called for updated
guidelines in 2011 aimed at answering 3 major
questions:
– Does initiating antihypertensive treatment at specific BP
thresholds improve health outcomes?
– Does treatment with antihypertensive therapy to a specific BP
goal improve health outcomes?
– Are there differences in benefit/harm between antihypertensive
drugs or drug classes on specific health outcomes?
6 December 2016 Kovell LC et al. J Am Heart Assoc. 2015;4(12): e002315
James PA et al. JAMA. 2014;311:507–20
48. No
No
No
Black
JNC 8 Hypertension Guideline
Algorithm
Lifestyle changes:
• SmokingCessation
• Control blood glucose andlipids
• Diet
Eat healthy (i.e., DASHdiet)
Moderate alcoholconsumption
Reduce sodium intake to
no more than 2,400
mg/day
• Physical activity
Moderate-to-vigorous
activity 3-4 days a week
averaging 40 min persession.
Adult aged ≥ 18 years with HTN
Implement lifestyle modifications
Set BP goal, initiate BP-lowering medication based on algorithm
General Population
(no diabetes or CKD) Diabetes or CKD present
Age ≥ 60 years Age < 60 years All Ages
Diabetes
present No CKD
All Ages and Races
CKD present with
or without diabetes
BP Goal
< 150/90
BP Goal
< 140/90
BP Goal
< 140/90
BP Goal
< 140/90
Nonblack
Yes
Initiate thiazide or
CCB, alone or
combo
Initiate ACEI or
ARB, alone or
combo
w/another class
Reinforce lifestyle and adherence
Add a medication class not already selected (i.e. beta blocker, aldosterone antagonist, others) and titrate
above medications to max (see back of card)
Initiate thiazide, ACEI, ARB,
or CCB, alone or in combo
Reinforce lifestyle and adherence
Titrate meds to maximum doses, add another med and/or refer to hypertension specialist
Yes
Continue tx and monitoring
Initial Drugs of Choice forHypertension
• ACE inhibitor (ACEI)
• Angiotensin receptor blocker (ARB)
• Thiazide diuretic
• Calcium channel blocker(CCB)
At blood pressure goal?
At blood pressure goal?
Reinforce lifestyle and adherence
Titrate medications to maximum doses or consider adding another medication (ACEI, ARB, CCB, Thiazide)
At blood pressure goal?
Yes
Strategy Description
A Start one drug, titrate to maximum
dose, and then add a seconddrug.
B Start one drug, then add a second
drug before achieving max dose of
first
C Begin 2 drugs at same time, as
separate pills or combination pill.
Initial combination therapy is
recommended if BP is greaterthan
20/10mm Hg abovegoal
Reference: James PA, Ortiz E, et al. 2014 evidence-based guideline for the management
of high blood pressure in adults: (JNC8). JAMA. 2014 Feb 5;311(5):507-20
Card developed by Cole Glenn, Pharm.D. & James L Taylor, Pharm.D.
49. CompellingIndications
Hypertension Treatment
Beta-1 Selective Beta-blockers – possibly safer in patients
with COPD, asthma, diabetes, and peripheral vascular
disease:
• metoprolol
• bisoprolol
• betaxolol
• acebutolol
Indication TreatmentChoice
Heart Failure ACEI/ARB + BB + diuretic + spironolactone
Post –MI/ClinicalCAD ACEI/ARB AND BB
CAD ACEI, BB, diuretic, CCB
Diabetes ACEI/ARB, CCB, diuretic
CKD ACEI/ARB
Recurrent stroke prevention ACEI, diuretic
Pregnancy labetolol (first line), nifedipine, methyldopa
Drug Class Agents of Choice Comments
Diuretics HCTZ 12.5-50mg, chlorthalidone 12.5-25mg, indapamide 1.25-2.5mg
triamterene 100mg
K+ sparing – spironolactone 25-50mg, amiloride 5-10mg, triamterene
100mg
furosemide 20-80mg twice daily, torsemide10-40mg
Monitor for hypokalemia
Most SE are metabolic in nature
Most effective when combined w/ ACEI
Stronger clinical evidence w/chlorthalidone
Spironolactone - gynecomastia and hyperkalemia
Loop diuretics may be needed when GFR<40mL/min
ACEI/ARB ACEI: lisinopril, benazapril, fosinopril and quinapril 10-40mg, ramipril5-
10mg, trandolapril2-8mg
ARB: candesartan 8-32mg, valsartan 80-320mg, losartan 50-100mg,
olmesartan 20-40mg, telmisartan20-80mg
SE: Cough (ACEI only), angioedema (more with ACEI),
hyperkalemia
Losartan lowers uric acid levels; candesartanmay
prevent migraineheadaches
Beta-Blockers metoprolol succinate 50-100mg and tartrate 50-100mg twice daily,
nebivolol 5-10mg, propranolol 40-120mg twice daily, carvedilol 6.25-25mg
twice daily, bisoprolol 5-10mg, labetalol 100-300mg twice daily,
Not first line agents – reserve for post-MI/CHF
Cause fatigue and decreased heartrate
Adversely affect glucose; mask hypoglycemic awareness
Calciumchannel
blockers
Dihydropyridines: amlodipine 5-10mg, nifedipine ER 30-90mg,
Non-dihydropyridines: diltiazem ER 180-360 mg, verapamil 80-120mg 3
times daily or ER 240-480mg
Cause edema; dihydropyridines may be safely combined
w/ B-blocker
Non-dihydropyridines reduce heart rate andproteinuria
Vasodilators hydralazine 25-100mg twice daily, minoxidil5-10mg
terazosin 1-5mg, doxazosin 1-4mg given at bedtime
Hydralazine and minoxidil may cause reflex tachycardia
and fluid retention – usually require diuretic +B-blocker
Alpha-blockers may cause orthostatichypotension
Centrally-acting
Agents
clonidine 0.1-0.2mg twice daily, methyldopa 250-500mg twicedaily
guanfacine 1-3mg
Clonidine available in weekly patch formulation for
resistant hypertension
50. JNC 8: Graded Recommendations
A – Strong evidence
B – Moderate evidence
C – Weak evidence
D – Against
E – Expert Opinion
N – No recommendation
51. JNC 8: Drug Treatment
Thresholds and Goals
Based on trials HYVET,Syst-Eur,SHEP, JATOS,VALISH,andCARDIO-SIS
Recommendation 1
• Age > 60 yrs
– Systolic:
• Threshold > 150 mmHg
• Goal < 150 mmHg
– LOE: Grade A
– Diastolic:
• Threshold > 90 mmHg
• Goal < 90 mmHg
– LOE: Grade A
52. JNC 8: Drug Treatment
Thresholds and Goals
• Age < 60 yrs
- Diastolic:
• Threshold > 90 mmHg
• Goal < 90 mmHg
– LOE: Grade A for ages 40-59; Grade E for ages 18-
39
– Systolic:
• Threshold > 140 mmHg
• Goal < 140 mmHg
– LOE: Grade E
(Trials HDFP,Hypertension-StrokeCooperative,MRC,ANBP,and
VA Cooperative)
Recommendation 2
Recommendation 3
53. JNC 8: Drug Treatment
Thresholds and Goals
Recommendation 4 & 5
• Age > 18 yrs with CKD or DM
– Systolic:
• Threshold > 140 mmHg
• Goal < 140 mmHg
– LOE: Grade E
– Diastolic:
• Threshold > 90 mmHg
• Goal < 90 mmHg
– LOE: Grade E
Quality evidencefrom3trials(SHEP,Syst-Eur, and UKPDS)
54. JNC 8: Initial Drug Choice
• Nonblack, including DM
– Thiazide diuretic, CCB, ACEI, ARB
• LOE: Grade B
• Black, including DM
– Thiazide diuretic, CCB
• LOE: Grade B (Grade C for diabetics)
Recommendation 6
Recommendation 7
3 federally funded trials (VA Cooperative Trial, HDFP, and SHEP)
55. JNC 8: Initial Drug Choice
Recommendation 8
• Age > 18 yrs with CKD and HTN
(regardless of race or diabetes)
– Initial (or add-on) therapy should include
an ACEI or ARB to improve kidney
outcomes
• LOE: Grade B
– Blacks w/ or w/o proteinuria
• ACEI or ARB as initial therapy (LOE: Grade E)
– No evidence for RAS-blockers > 75 yo
• Diuretic is an option for initial therapy
From trial The AASK study
56. JNC 8: Subsequent Management
Recommendation 9
• Reassess treatment monthly
• Avoid ACEI/ARB combination
• Consider 2-drug initial therapy for
Stage 2 HTN (> 160/100)
• Goal BP not reached with 3 drugs, use
drugs from other classes
– LOE: Grade E
63. Pregnant women
•
•
•
•
If BP > 160/110 mmHg, treatment is
recommended (I, C).
Consider drug Rx (IIb, C)
– BP ≥150/95mmHg, or
– BP ≥140/90 mmHg + TOD
Methyldopa, labetolol, nifedipine preferred
(IIa, B)
Pre-eclampsia: IV labetolol or nitroprusside
(IIa, B)
64. DM
• Start drug Rx when SBP ≥140 mmHg (I, A).
• Target SBP < 140/90 mmHg (I, A).
• All classes of drugs are recommended and
can be used (I, A).
• RAS blockers preferred, especially if having
proteinuria / microalbuminuria (I, A).
65. HT with nephropathy
•
•
•
•
•
Target SBP < 140 mmHg (IIa, B).
RAS blockers indicated for HT with overt proteinuria
or microalbuminuria (I, A).
Recommend combining RAS blockers with other
anti-HT drugs to achieve target BP (I, A).
Combining two RAS blockers is not recommended
(III, A).
Aldosterone antagonists not recommened in CKD
(III, C).
67. Atherosclerosis, arteriosclerosis, peripheral
artery disease
• Target BP < 140/90 mmHg.
• Carotid atherosclerosis: CCB, ACEI (IIa, B).
• PAD: BB may be considered. Their use does
not appear to be associated with worsening
of PAD symptoms (IIIb, A).
68. Resistant Hypertension
• Blood pressure remaining above goal (150/90 mm
Hg for the overall population and 140/90 mm Hg for
those with DM or CKD) in spite of concurrent use of
3 antihypertensive agents of different classes.
• Ideally, 1 of the 3 agents should be a diuretic & all
agents should be prescribed at optimal dose
amounts.
The JNC 7 report. JAMA 2003; 289: 2560-72.
69. Resistant HT
• MR antagonist, amiloride, doxazosin should
be considered.
• If drugs are ineffective: renal denervation and
baroreceptor stimulation may be considered
(IIb, C) (only by experienced operators at
restricted HT centers).
70. Conclusion
•
•
•
•
Patients with DM & CKD require more aggressive BP
control.
Most patients with hypertension will require two or
more antihypertensive medications to control blood
pressure.
The use of combination therapy is appropriate as
initial treatment.
Sustained antihypertensive efficacy may protect
against the early morning rise in blood pressure that
leads to heightened risk of cardiovascular events.
1. Kearney PM, Whelton M, Reynolds K, Muntner P, Whelton PK, He J. Global burden of hypertension: analysis of worldwide data. Lancet. 2005 Jan 15-21;365(9455):217-23.
2. Gaziano TA, Asaf B, S Anand, et.al. The global cost of nonoptimal blood pressure. J Hypertens 2009; 27(7): 1472-1477.